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Disease Ontology Browser
Weyers acrofacial dysostosis (DOID:0111571)
Alliance: disease page
Synonyms: acrofacial dysostosis, Weyers type; Curry-Hall syndrome; WAD; Weyers acrodental dysostosis
Alt IDs: OMIM:193530, MESH:C536695, ORDO:952, UMLS_CUI:C0457013
Definition: An acrofacial dysostosis characterized by dental anomalies, nail dystrophy, postaxial polydactyly, and mild short stature that has_material_basis_in heterozygous mutation in the genes EVC2 or EVC on chromosome 4p16.2.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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12/10/2024
MGI 6.24 		The Jackson Laboratory